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Ibuprofen and Pseudoephedrine Hydrochloride

NDC 51660-490 · HUMAN OTC DRUG · TABLET, SUGAR COATED

Labeler / ManufacturerOhm Laboratories Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074567
Dosage form / routeTABLET, SUGAR COATED · ORAL
Active ingredientsIBUPROFEN (200 mg/1)
PSEUDOEPHEDRINE HYDROCHLORIDE (30 mg/1)
Marketing started20011013
Package count1

External sources

Source: openFDA. Public-domain (CC0).